Canonical Allele Identifier: CA1229578299

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502856C= , CM000663.2:g.241502856C=	GRCh38
NC_000001.10:g.241666156C= , CM000663.1:g.241666156C=	GRCh37
NC_000001.9:g.239732779C=	NCBI36
NG_012338.1:g.21899G= , LRG_504:g.21899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1612-286G=
ENST00000682162.1:c.1138-286G=	ENSP00000508203.1:n.1138-286G=
ENST00000682567.1:n.2371G=
ENST00000683521.1:c.1109-286G=	ENSP00000506864.1:n.1109-286G=
ENST00000684161.1:n.2324-286G=
ENST00000684483.1:c.*505-286G=	ENSP00000507894.1:n.*505-286G=
ENST00000366560.4:c.1109-286G= MANE Select	ENSP00000355518.4:n.1109-286G=
ENST00000366560.3:c.1109-286G=	ENSP00000355518.3:n.1109-286G=
NM_000143.3:c.1109-286G= , LRG_504t1:c.1109-286G=	NP_000134.2:n.1109-286G=
XM_011544132.1:c.881-286G=	XP_011542434.1:n.881-286G=
XM_011544132.2:c.881-286G=	XP_011542434.1:n.881-286G=
NM_000143.4:c.1109-286G= MANE Select	NP_000134.2:n.1109-286G=